# K070562: EZ Plus Implant System

- Pathway: 510(k) (Traditional)
- Applicant: Megagen Co., Ltd.
- Decided: May 18, 2007 after 80 days
- Product code: NHA (Abutment, Implant, Dental, Endosseous)
- Device class: 2
- Regulation: 21 CFR 872.3630
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 7 generations back to K944964 (1995). 54 ancestors in all.
74 later devices descend from it; 6 cite it directly.
0 of 129 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K052369: Exfeel Implant System, Megagen Co., Ltd. (2006) Summary page 1.

## Most influential descendants
- K110955: Anyridge Internal Implant System (2011), 43 descendants of its own
- K122231: Xpeed Any Ridge Internal Implant System (2012), 25 descendants of its own
- K073486: Dentis Dental Implant System (2008), 25 descendants of its own
- K150344: Dentis Dental Implant System (2015), 20 descendants of its own
- K123988: Anyonetm Internal Implant System (2013), 19 descendants of its own

## Indications for use
The EZ Plus Implant Systems are intended to be surgically placed in the upper or lower jaw to support prosthetic devices, such as artificial teeth, and to restore a patient's chewing function. This may be accomplished using either a two stage surgical procedure or a single stage surgical procedure. Large angle abutments (e.g. 250) on small diameter implants of the EZ Plus internal connection system are intended for the anterior region of the mouth and not intended for use in the posterior region of the mouth due to limited strength of the implant.

Source page: https://510kreport.com/device/K070562
Methodology: https://510kreport.com/methodology